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Phosphorus tribromide → 1-(Bromomethyl)-2,3,5-triiodobenzene

HRID 58355
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HRID 58355 반응식
P(Br)(Br)[Br:2].[I:5][C:6]1[C:13]([I:14])=[CH:12][C:11]([I:15])=[CH:10][C:7]=1[CH2:8]O.O.C(Cl)Cl>O1CCCC1>[I:5][C:6]1[C:13]([I:14])=[CH:12][C:11]([I:15])=[CH:10][C:7]=1[CH2:8][Br:2]
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참가 물질

5

반응물 3

HCID 24614Phosphorus tribromideHCID 34957432,3,5-Triiodobenzyl alcoholHCID 21908982Water methylene chloride

생성물 1

HCID 534030771-(Bromomethyl)-2,3,5-triiodobenzene수율 85.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

A solution of phosphorous tribromide (3.8 ml, 40 mmol) was added dropwise to a solution of 2,3,5-triiodobenzyl alcohol 1 (9.72 g, 20 mmol) in dry tetrahydrofuran (50 ml) at 0° C. under dry nitrogen gas flow. The reaction mixture was stirred 5 minutes at 0° C., then 20 minutes at room temperature (18° C.), then cold H2O/DCM (60160 ml) was added. The resulting aqueous phase was extracted with dichloromethane (2×10 ml). The combined organic extracts were washed with NaHCO3 aq (20 ml) and H2O (20 ml) then dried (Na2SO4), filtered and concentrated. The white solid was also washed with cold methanol (45 ml). 9.35 g of 2,3,5-triiodobenzyl bromide in the form of a white clean solid was obtained in 85% yield.

후처리

  1. extractionThe resulting aqueous phase was extracted with dichloromethane (2×10 ml)
  2. washThe combined organic extracts were washed with NaHCO3 aq (20 ml) and H2O (20 ml)
  3. dry with materialthen dried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. washThe white solid was also washed with cold methanol (45 ml)

출처 및 근거

ORD 기록
ord-4346e0a624cc4077a7a9da9db4c8f90a
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434800B2

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